Quality Assurance Specialist

Novartis ACC; Zaragoza; Presencial; EUR 40.000 - 55.000; Jornada completa

Descripción de la vacante

A global healthcare company in Zaragoza seeks a Compliance Specialist responsible for ensuring adherence to regulatory standards and quality systems. The ideal candidate will have a Bachelor's degree in Pharmacy and at least 2 years in pharmaceutical operations, with strong communication skills in English and Spanish. This role involves collaboration for audit preparation and supporting quality management processes to maintain compliance. Join us to contribute to our mission of improving lives through innovative medicines.

Formación

• 2+ years of experience in a GxP (Bio)pharmaceutical or API manufacturing operations.
• 1+ years of experience in a Quality Assurance role.
• Excellent communication skills in English and Spanish.

Responsabilidades

• Collaborates to ensure compliance with regulatory and GMP standards.
• Provides oversight for the implementation of Quality Systems.
• Supports the quality management in audit and inspection readiness.

Conocimientos

Communication skills

Fluent English

Fluent Spanish

Educación

Bachelor's Degree in Pharmacy

MSc in Pharmaceutical Industry

Descripción del empleo

Summary

The Compliance specialist is responsible to collaborate with relevant manager for maintaining and developing the quality systems strategy, policies, processes, standards and procedures to ensure the site complies with regulatory and GMP compliance requirements as described by authorities and by Novartis/Adacap guidelines and quality manual.

The function supports the manager to guarantee that global procedures are implemented in the site’s quality systems and challenges the system for further improvement. The function supports in the site’s inspection readiness and is a key contributor of the inspection management program.

About The Role

Major Accountabilities

• Collaborates to ensure that the site’s quality system is maintained compliant to regulatory and GMP compliance requirements.
• Collaborates in the management of the site’s quality systems documentation and reviews, defines updates and approves (when agreed with the quality management) site specific quality systems documents.
• Provides oversight for the implementation of Quality Systems and Regulatory Compliance including management of Non conformances, CAPAs, Effectiveness Checks, Change Controls, Training, Inspections and Audit readiness, Technical complaints, Risk Assessments and remediation, Annual Product Quality review, self-assessments, KPIs and Quality Management
• Review.
• Support the manager in the design and oversight of strategic site quality system and works in collaboration with site functions to define written procedures including but not limited to monitor and control of the manufacturing environment, training, document control/record retention, deviations/CAPA investigations, and monitoring compliance with all requirements of good
• manufacturing practice.
• Support the quality management to develop and deliver a robust overall quality system, strategy, and ultimate plan resulting in a fully compliant quality system infrastructure with respect to procedures and processes.
• Provides oversight for audit and inspection management, inspection strategies, preparation, interactions and responses.
• Support the quality team in the health authority inspection preparation and ensures key support during MOH and Novartis global audits.
• Develop Health Authority communications, including written correspondence,
• responses to inspection observations, presentations and verbal communication
• Works with quality and compliance team to ensure robust quality systems are implemented and
• sustained including, deviation/CAPA Management: Ensures all deviations from established
• procedures are appropriately documented and investigated to determine and fix root cause.
• Support escalation of Quality/cGMP issues and deficiencies to the Site QA Head and support global escalation process if needed. Support associates within the Novartis network incase of Health Authority Notifications (s.a. FAR, Rapid alert, recalls)

Minimum Requirements

• Education: Bachelor´s Degree in Pharmacy or MSc in Pharmaceutical Industry.
• 2+ years of experience in a GxP (Bio)pharmaceutical or API manufacturing operations up of which 1+ years of experience in a Quality Assurance role.
• Excellent communication skills
• Fluent English and Spanish, written and spoken.

Why Novartis?

Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards

Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

Commitment to Diversity And Inclusion

Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Why Novartis

Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards

Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards